| Literature DB >> 18292808 |
Laura A Napolitano1, Diane Schmidt, Michael B Gotway, Niloufar Ameli, Erin L Filbert, Myra M Ng, Julie L Clor, Lorrie Epling, Elizabeth Sinclair, Paul D Baum, Kai Li, Marisela Lua Killian, Peter Bacchetti, Joseph M McCune.
Abstract
Growth hormone (GH) is an underappreciated but important regulator of T cell development that can reverse age-related declines in thymopoiesis in rodents. Here, we report findings of a prospective randomized study examining the effects of GH on the immune system of HIV-1-infected adults. GH treatment was associated with increased thymic mass. In addition, GH treatment enhanced thymic output, as measured by both the frequency of T cell receptor rearrangement excision circles in circulating T cells and the numbers of circulating naive and total CD4(+) T cells. These findings provide compelling evidence that GH induces de novo T cell production and may, accordingly, facilitate CD4(+) T cell recovery in HIV-1-infected adults. Further, these randomized, prospective data have shown that thymic involution can be pharmacologically reversed in humans, suggesting that immune-based therapies could be used to enhance thymopoiesis in immunodeficient individuals.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18292808 PMCID: PMC2248326 DOI: 10.1172/JCI32830
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808